首页> 外文期刊>Nature biotechnology >Advancing RNA-Seq analysis.Comments Comment on: Nat Biotechnol. 2010 May;28(5):503-10; PMID: 20436462, Comment on: Nat Biotechnol. 2010 May;28(5):511-5; PMID: 20436464
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Advancing RNA-Seq analysis.Comments Comment on: Nat Biotechnol. 2010 May;28(5):503-10; PMID: 20436462, Comment on: Nat Biotechnol. 2010 May;28(5):511-5; PMID: 20436464

机译:先进的RNA序列分析评论评论:Nat Biotechnol。 2010 May; 28(5):503-10; PMID:20436462,评论:Nat Biotechnol。 2010 May; 28(5):511-5; PMID:20436464

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摘要

Sequencing of RNA has long been recognized as an efficient method for gene discovery1 and remains the gold standard for annotation of both coding and noncoding genes2. Compared with earlier methods, massively parallel sequencing of RNA (RNA-Seq)3 has vastly increased the throughput of RNA sequencing and allowed global measurement of transcript abundance. Two reports in this issue introduce approaches for RNA-Seq analysis that capture genome-wide transcription and splicing in unprecedented detail. Trapnell et al.4 describe a software package, Cufflinks, for simultaneous discovery of transcripts and quantification of expression levels and apply it to study gene expression and splicing during the differentiation of mouse myoblast cells. Taking a similar approach, Guttman et al.5 use software called Scripture to reannotate the transcriptomes of three mouse cell lines, defining complete gene models for hundreds of new large intergenic noncoding RNAs (lincRNAs).
机译:长期以来,RNA测序一直被认为是一种有效的基因发现方法,1仍然是注释编码和非编码基因的黄金标准2。与早期方法相比,RNA的大规模并行测序(RNA-Seq)3大大提高了RNA测序的通量,并允许对转录本丰度进行整体测量。本期的两份报告介绍了用于RNA-Seq分析的方法,该方法捕获了全基因组范围的转录和剪接,其作用前所未有。 Trapnell等人4描述了一个软件包Cufflinks,用于同时发现转录本和定量表达水平,并将其用于研究小鼠成肌细胞分化过程中的基因表达和剪接。 Guttman等人[5]采用类似的方法,使用称为Scripture的软件来重新注释三种小鼠细胞系的转录组,从而定义了数百种新的大型基因间非编码RNA(lincRNA)的完整基因模型。

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